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Isolation, identification and utilization of lactic acid bacteria from silage in a warm and humid climate area

The study aimed to isolate and identify lactic acid bacteria (LAB) from silages and their application to improve the fermentation quality of alfalfa. Forty-nine LAB strains were isolated from silages, and two strains were screened for growth and acid production rates. Then two strains were selected...

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Autores principales: Peng, Chao, Sun, Wentao, Dong, Xiang, Zhao, Lili, Hao, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8206206/
https://www.ncbi.nlm.nih.gov/pubmed/34131227
http://dx.doi.org/10.1038/s41598-021-92034-0
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author Peng, Chao
Sun, Wentao
Dong, Xiang
Zhao, Lili
Hao, Jun
author_facet Peng, Chao
Sun, Wentao
Dong, Xiang
Zhao, Lili
Hao, Jun
author_sort Peng, Chao
collection PubMed
description The study aimed to isolate and identify lactic acid bacteria (LAB) from silages and their application to improve the fermentation quality of alfalfa. Forty-nine LAB strains were isolated from silages, and two strains were screened for growth and acid production rates. Then two strains were selected for Physiological and morphological tests and 16S rRNA sequencing. They were Gram-positive and Catalase-negative and were able to grow at pH 3.5 and at 45 °C, were unable to grow different NaCl concentrations as 3.0% and 6.5%. Strain BDy3-10 was identified as Lactobacillus rhamnosus, while TSy1-3 was identified as L. buchneri. The selected strains were evaluated on fermentation of alfalfa silage. The highest crude protein content occurred in the BDy3-10 treatment group. The contents of neutral detergent fiber and acid detergent fiber in the TSy1-3 treatment were significantly lower than other treatment (P < 0.05). Compared to the control treatment, inoculation treatments deceased pH during ensiling (P < 0.001) and provided the most increased lactic acid content after ensiling for 10 days (P < 0.001). The acetic acid contents of all the inoculation groups were significantly increased (P < 0.001) during ensiling, and were lower than that of control group (P < 0.001). So, the TSy1-3 treatment most effectively improved the fermentation quality of alfalfa silage in warm and humid climate area.
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spelling pubmed-82062062021-06-16 Isolation, identification and utilization of lactic acid bacteria from silage in a warm and humid climate area Peng, Chao Sun, Wentao Dong, Xiang Zhao, Lili Hao, Jun Sci Rep Article The study aimed to isolate and identify lactic acid bacteria (LAB) from silages and their application to improve the fermentation quality of alfalfa. Forty-nine LAB strains were isolated from silages, and two strains were screened for growth and acid production rates. Then two strains were selected for Physiological and morphological tests and 16S rRNA sequencing. They were Gram-positive and Catalase-negative and were able to grow at pH 3.5 and at 45 °C, were unable to grow different NaCl concentrations as 3.0% and 6.5%. Strain BDy3-10 was identified as Lactobacillus rhamnosus, while TSy1-3 was identified as L. buchneri. The selected strains were evaluated on fermentation of alfalfa silage. The highest crude protein content occurred in the BDy3-10 treatment group. The contents of neutral detergent fiber and acid detergent fiber in the TSy1-3 treatment were significantly lower than other treatment (P < 0.05). Compared to the control treatment, inoculation treatments deceased pH during ensiling (P < 0.001) and provided the most increased lactic acid content after ensiling for 10 days (P < 0.001). The acetic acid contents of all the inoculation groups were significantly increased (P < 0.001) during ensiling, and were lower than that of control group (P < 0.001). So, the TSy1-3 treatment most effectively improved the fermentation quality of alfalfa silage in warm and humid climate area. Nature Publishing Group UK 2021-06-15 /pmc/articles/PMC8206206/ /pubmed/34131227 http://dx.doi.org/10.1038/s41598-021-92034-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Peng, Chao
Sun, Wentao
Dong, Xiang
Zhao, Lili
Hao, Jun
Isolation, identification and utilization of lactic acid bacteria from silage in a warm and humid climate area
title Isolation, identification and utilization of lactic acid bacteria from silage in a warm and humid climate area
title_full Isolation, identification and utilization of lactic acid bacteria from silage in a warm and humid climate area
title_fullStr Isolation, identification and utilization of lactic acid bacteria from silage in a warm and humid climate area
title_full_unstemmed Isolation, identification and utilization of lactic acid bacteria from silage in a warm and humid climate area
title_short Isolation, identification and utilization of lactic acid bacteria from silage in a warm and humid climate area
title_sort isolation, identification and utilization of lactic acid bacteria from silage in a warm and humid climate area
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8206206/
https://www.ncbi.nlm.nih.gov/pubmed/34131227
http://dx.doi.org/10.1038/s41598-021-92034-0
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